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dc.contributor.authorSaint-André, Violaine
dc.contributor.authorFederation, Alexander J.
dc.contributor.authorLin, Charles Y.
dc.contributor.authorAbraham, Brian J.
dc.contributor.authorLee, Tong Ihn
dc.contributor.authorBradner, James E.
dc.contributor.authorReddy, Jessica
dc.contributor.authorYoung, Richard A.
dc.date.accessioned2017-04-12T20:27:41Z
dc.date.available2017-04-12T20:27:41Z
dc.date.issued2016-03
dc.date.submitted2015-08
dc.identifier.issn1088-9051
dc.identifier.issn1549-5469
dc.identifier.urihttp://hdl.handle.net/1721.1/108087
dc.description.abstractA small set of core transcription factors (TFs) dominates control of the gene expression program in embryonic stem cells and other well-studied cellular models. These core TFs collectively regulate their own gene expression, thus forming an interconnected auto-regulatory loop that can be considered the core transcriptional regulatory circuitry (CRC) for that cell type. There is limited knowledge of core TFs, and thus models of core regulatory circuitry, for most cell types. We recently discovered that genes encoding known core TFs forming CRCs are driven by super-enhancers, which provides an opportunity to systematically predict CRCs in poorly studied cell types through super-enhancer mapping. Here, we use super-enhancer maps to generate CRC models for 75 human cell and tissue types. These core circuitry models should prove valuable for further investigating cell-type–specific transcriptional regulation in healthy and diseased cells.en_US
dc.description.sponsorshipUnited States. National Institutes of Health (HG002668)en_US
dc.language.isoen_US
dc.publisherCold Spring Harbor Laboratory Pressen_US
dc.relation.isversionofhttp://dx.doi.org/10.1101/gr.197590.115en_US
dc.rightsThis article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.en_US
dc.sourceCold Spring Harbor Laboratory Pressen_US
dc.titleModels of human core transcriptional regulatory circuitriesen_US
dc.typeArticleen_US
dc.identifier.citationSaint-André, Violaine, Alexander J. Federation, Charles Y. Lin, Brian J. Abraham, Jessica Reddy, Tong Ihn Lee, James E. Bradner, and Richard A. Young. “Models of Human Core Transcriptional Regulatory Circuitries.” Genome Res. 26, no. 3 (February 3, 2016): 385–396.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorReddy, Jessica
dc.contributor.mitauthorYoung, Richard A
dc.relation.journalGenome Researchen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsSaint-André, Violaine; Federation, Alexander J.; Lin, Charles Y.; Abraham, Brian J.; Reddy, Jessica; Lee, Tong Ihn; Bradner, James E.; Young, Richard A.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-2171-9394
dc.identifier.orcidhttps://orcid.org/0000-0001-8855-8647
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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